| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304334.1 | 630 | Missense Mutation | AGG,TGG | R135W | NP_001291263.1 |
| NM_001304335.1 | 630 | Intron | NP_001291264.1 | ||
| NM_001304336.1 | 630 | UTR 3 | NP_001291265.1 | ||
| NM_001304337.1 | 630 | Intron | NP_001291266.1 | ||
| NM_198542.2 | 630 | Missense Mutation | AGG,TGG | R136W | NP_940944.1 |